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Sorption Properties (sorption + property)
Selected AbstractsA Simple Lithium(I) Salt with a Microporous Structure and Its Gas Sorption Properties,ANGEWANDTE CHEMIE, Issue 6 2010Brendan Aufnahmefähig: Durch Kombination von Lithium-Kationen mit Isonicotinat- Anionen (1) erhält man ein Salz (siehe Bild; C,schwarz, O,rot, N,blau, Li,violett), das H2,, N2,, CO2 und CH4 reversibel aufnehmen und abgeben kann. Der Festkörper liegt als dreidimensionales Gerüst vor, in dessen Mikrokanälen sich Lösungsmittelmoleküle befinden. [source] Hydrogen Sorption Properties of Mg,1 wt.% Ni,0.2 wt.% Pd Prepared by Reactive Milling.CHEMINFORM, Issue 11 2006O. Gutfleisch Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF. [source] Sorption properties of the iminodiacetate ion exchange resin, amberlite IRC-718, toward divalent metal ionsJOURNAL OF APPLIED POLYMER SCIENCE, Issue 2 2008Charef Noureddine Abstract The sorption properties of the commercially available cationic exchange resin, Amberlite IRC-718, that has the iminodiacetic acid functionality, toward the divalent metal-ions, Fe2+, Cu2+, Zn2+, and Ni2+ were investigated by a batch equilibration technique at 25°C as a function of contact time, metal ion concentration, mass of resin used, and pH. Results of the study revealed that the resin exhibited higher capacities and a more pronounced adsorption toward Fe2+ and that the metal-ion uptake follows the order: Fe2+ > Cu2+> Zn2+ >Ni2+. The adsorption and binding capacity of the resin toward the various metal ions investigated are discussed. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci, 2008 [source] Evaluation of sorbent amendments for in situ remediation of metal-contaminated sedimentsENVIRONMENTAL TOXICOLOGY & CHEMISTRY, Issue 9 2010Seokjoon Kwon Abstract The present study evaluated sorbent amendments for in situ remediation of sediments contaminated with two divalent metals. A literature review screening was performed to identify low-cost natural mineral-based metal sorbents and high-performance commercial sorbents that were carried forward into laboratory experiments. Aqueous phase metal sorptivity of the selected sorbents was evaluated because dissolved metals in sediment porewater constitute an important route of exposure to benthic organisms. Based on pH-edge sorption test results, natural sorbents were eliminated due to inferior performance. The potential as in situ sediment amendment was explored by comparing the sorption properties of the engineered amendments in freshwater and saltwater (10 PPT salinity estuarine water) matrices. Self-assembled monolayers on mesoporous supports with thiols (Thiol-SAMMSÔ) and a titanosilicate mineral (ATSÔ) demonstrated the highest sorption capacity for cadmium (Cd) and lead (Pb), respectively. Sequential extraction tests conducted after mixing engineered sorbents with contaminated sediment demonstrated transfer of metal contaminants from a weakly bound state to a more strongly bound state. Biouptake of Cd in a freshwater oligochaete was reduced by 98% after 5-d contact of sediment with 4% Thiol-SAMMS and sorbed Cd was not bioavailable. While treatment with ATS reduced the small easily extractable portion of Pb in the sediment, the change in biouptake of Pb was not significant because most of the native lead was strongly bound. The selected sorbents added to sediments at a dose of 5% were mostly nontoxic to a range of sensitive freshwater and estuarine benthic organisms. Metal sorbent amendments in conjunction with activated carbon have the potential to simultaneously reduce metal and hydrophobic contaminant bioavailability in sediments. Environ. Toxicol. Chem. 2010;29:1883,1892. © 2010 SETAC [source] Modelling of colloid leaching from unsaturated, aggregated soilEUROPEAN JOURNAL OF SOIL SCIENCE, Issue 3 2007M. Laegdsmand Summary The migration of colloids in soils can enhance the leaching of strongly sorbing contaminants. We present a model for the simulation of colloid leaching from unsaturated, aggregated soil media under stationary flow. Transport in the intra-aggregate pores is simulated by convection,dispersion, and transport in the interaggregate pores, and a stagnant layer of water surrounding the aggregates, is simulated by diffusion. The model describes the release of colloids from soil aggregates, sorption and desorption processes at the air,water interfaces, and flocculation and subsequent straining from the flowing water. All three processes were simulated as functions of ionic strength. Transport of ions in intra-aggregate pores was simulated by Fickian diffusion. The model was calibrated against experimental results of colloid leaching from columns packed with natural soil aggregates. The aggregates were of two soils differing in organic matter content. On each soil a single calibrated parameter set could describe the experiments with the three ionic strengths. The parameters for release of colloids from the aggregate surface and the sorption properties of the air,water interface were different for the two soils. The key parameters for leaching were the thickness of the stagnant layer of water surrounding the aggregates, the mechanical dispersion, the maximum concentration of colloids at the surface of the aggregates, the sorption capacity and rate coefficient of the colloids at the air,water interface, and the colloid diffusion coefficient. Simulations were also done with two additional irrigation intensities at one ionic strength. Simulated leaching was greater than measured leaching at both irrigation intensities, but the diffusion-controlled release of colloids from the aggregates was simulated correctly. [source] Porous Chromium Terephthalate MIL-101 with Coordinatively Unsaturated Sites: Surface Functionalization, Encapsulation, Sorption and CatalysisADVANCED FUNCTIONAL MATERIALS, Issue 10 2009Do-Young Hong Recent ideas concerning site-selective functionalization of chromium terephtha-late MIL-101 are discussed, focusing on the utilization of unsaturated Cr(III) sites (see image). Recent advances in synthesis, selective surface functionalization, outstanding sorption properties, encapsulation of nanoobjects, and catalytic applications in MIL-101 are also discussed. [source] Microporous Metal,Organic Frameworks with High Gas Sorption and Separation Capacity,ADVANCED FUNCTIONAL MATERIALS, Issue 8 2007Y. Lee Abstract The design, synthesis, and structural characterization of two microporous metal,organic framework structures, [M(bdc)(ted)0.5]·2,DMF·0.2,H2O (M,=,Zn (1), Cu (2); H2bdc,=,1,4-benzenedicarboxylic acid; ted,=,triethylenediamine; DMF: N,N -dimethylformamide) is reported. The pore characteristics and gas sorption properties of these compounds are investigated at cryogenic temperatures, room temperature, and higher temperatures by experimentally measuring argon, hydrogen, and selected hydrocarbon adsorption/desorption isotherms. These studies show that both compounds are highly porous with a pore volume of 0.65 (1) and 0.52,cm3,g,,1 (2). The amount of the hydrogen uptake, 2.1,wt,% (1) and 1.8,wt,% (2) at 77,K (1,atm; 1,atm,=,101,325,Pa), places them among the group of metal,organic frameworks (MOFs) having the highest H2 sorption capacity. [Zn(bdc)(ted)0.5]·2,DMF·0.2,H2O adsorbs a very large amount of hydrocarbons, including methanol, ethanol, dimethylether (DME), n -hexane, cyclohexane, and benzene, giving the highest sorption values among all metal,organic based porous materials reported to date. In addition, these materials hold great promise for gas separation. [source] Effect of molecular weight, temperature, and additives on the moisture sorption properties of polyethylene glycolJOURNAL OF PHARMACEUTICAL SCIENCES, Issue 1 2010Jared A. Baird Abstract Polyethylene glycol (PEG) is a hygroscopic polymer that undergoes the phenomenon of deliquescence once a critical relative humidity (RH0) is reached. The purpose of this study was to test the hypothesis that the deliquescence behavior of PEG will be affected by the polymer molecular weight, temperature, and the presence of additives. The deliquescence relative humidity for single component (RH0) and binary mixtures (RH0,mix) were measured using an automated gravimetric moisture analyzer at 25 and 40°C. Changes in PEG crystallinity after exposure to moisture were qualitatively assessed using powder X-ray diffraction (PXRD). Optical microscopy was used to visually observe the deliquescence phenomenon. For single component systems, decreasing PEG MW and elevating the temperature resulted in a decrease in the observed RH0. Physical mixtures of acetaminophen and anhydrous citric acid with both PEG 3350 and PEG 100,000 exhibited deliquescence (RH0,mix) at a relative humidity below that of either individual component. Qualitative changes in crystallinity were observed from the X-ray diffractograms for each PEG MW grade at high relative humidities, indicating that phase transformation (deliquescence) of the samples had occurred. In conclusion, it was found that the deliquescence behavior of PEG was affected by the polymer MW, temperature, and the presence of additives. This phenomenon may have important implications for the stability of PEG containing formulations. © 2009 Wiley-Liss, Inc. and the American Pharmacists Association J Pharm Sci 99:154,168, 2010 [source] Detection of NH3 by Quartz Crystal Microbalance Coated with Ta2O5PLASMA PROCESSES AND POLYMERS, Issue 2 2006Velichka Georgieva Abstract Summary: This paper reports a study of the sorption properties of thin Ta2O5 films to NH3 vapors. The films are deposited using electron beam evaporation. In order to determine the sorption ability of Ta2O5 to NH3, a quartz crystal microbalance (QCM) with a thin Ta2O5 film is investigated. The Ta2O5 film is used as a receptor for the NH3 gas. The AT-cut, 14 MHz quartz resonators allow conversion of the additional mass loading that occurs as a result of sorption into a frequency shift. The experiments are carried out by measuring the resonant frequency shift of the QCM to vapors from an aqueous solution of NH3 with different concentrations from 10 to 10,000 ppm. The obtained experimental results indicate that the variations of the resonant frequency are a function of the ammonia concentration and the thickness of the Ta2O5 layer. The process of sorption is found to be reversible. The reported investigation shows that a QCM covered with a thin Ta2O5 layer is sensitive to ammonia vapors at room temperature and is able to detect NH3 concentrations in the investigated range (10,10,000 ppm). Relative change of QCM frequency versus ammonia concentration [source] A new composite sorbent for water and dye uptake: Highly swollen acrylamide/2-acrylamido-2-methyl-1-propanesulfonic acid/clay hydrogels crosslinked by 1,4-butanediol dimethacrylatePOLYMER COMPOSITES, Issue 1 2009Semiha Kundakci A novel type of highly swollen hydrogels based on acrylamide (AAm) with 2-acrylamido-2-methyl-1-propanesulfonic acid (AMPS) and clay such as bentonite (Bent) crosslinked by 1,4-butanediol dimethacrylate (BDMA) was prepared by free radical solution polymerization in aqueous media. Water uptake and dye sorption properties of polyelectrolyte AAm/AMPS hydrogels and AAm/AMPS/Bent composite hydrogels were investigated as a function of composition to find materials with swelling and sorption properties. FTIR analyses were made. Swelling experiments were performed in water and dye solution at 25°C, gravimetrically. Highly swollen AAm/AMPS and AAm/AMPS/Bent hydrogels were used in experiments on sorption of water-soluble monovalent cationic dye such as Lauths violet "LV, (Thionin)." Swelling of AAm/AMPS hydrogels was increased up to 1,920,9,222% in water and 867,4,644% in LV solutions, while AAm hydrogels swelled 905% in water and swelling of AAm/AMPS/Bent hydrogels was increased up to 2,756,10,422% in water and 1,200,3,332% in LV solutions, while AAm/Bent hydrogels swelled 849% in water. Some swelling kinetic and diffusional parameters were found. Water and LV diffusion into hydrogels was found to be non-Fickian in character. For sorption of cationic dye, LV into AAm/AMPS and AAm/AMPS/Bent hydrogel was studied by batch sorption technique at 25°C. The amount of the dye sorbed per unit mass removal effiency and partition coefficient of the hydrogels was investigated. The influence of AMPS content in the hydrogels to sorption was examined. POLYM. COMPOS., 2009. © 2008 Society of Plastics Engineers [source] Influence of chitosan characteristics on polymer properties.POLYMER INTERNATIONAL, Issue 2 2003I: Crystallographic properties Abstract The properties of chitosan depend on several parameters including its origin (shrimp, squid, fungi etc), characteristics (mol fraction of N -acetylation; molecular weight) and treatments used to condition it (dissolving, precipitation, drying). These parameters can influence the material's sorption properties for metal ions. It has been suggested that the changes in sorption properties are related to the crystallinity of the material. The present work focuses on the study of the crystallographic properties of samples prepared from shrimp, squid and fungi sources, with different characteristics and conditioned by several physical treatments (dissolving, reprecipitation and drying, including oven-drying, freeze-drying), prior to subsequent studies of their sorption properties for platinum (discussed in Part II of this manuscript). © 2003 Society of Chemical Industry [source] | |||||||||||||